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B 细胞前体急性淋巴细胞白血病患儿中 ETV6/CBFA2(TEL/AML1)融合基因与核型异常的相关性

Correlation between the ETV6/CBFA2 (TEL/AML1) fusion gene and karyotypic abnormalities in children with B-cell precursor acute lymphoblastic leukemia.

作者信息

Fears S, Vignon C, Bohlander S K, Smith S, Rowley J D, Nucifora G

机构信息

Department of Molecular Genetics and Cellular Biology, University of Chicago, Illinois, USA.

出版信息

Genes Chromosomes Cancer. 1996 Oct;17(2):127-35. doi: 10.1002/(SICI)1098-2264(199610)17:2<127::AID-GCC8>3.0.CO;2-7.

Abstract

The recently identified ETV6/CBFA2 (formerly known as TEL/AML1) fusion gene occurs as a result of the t(12;21)(p12;q22). Initial reports have indicated that the fusion transcript occurs in up to 30% of children diagnosed with B-cell precursor (CD10+, CD19+) acute lymphoblastic leukemia (ALL). In order to characterize the incidence of the t(12;21) at both the chromosomal level as well as the RNA transcript level, we have used a combination of classical cytogenetics, reverse transcriptase-polymerase chain reaction (RT-PCR), and fluorescence in situ hybridization (FISH) to examine the bone marrow of 34 children diagnosed with B-cell precursor ALL. Nine of the 34 patient samples expressed the ETV6/CBFA2 transcript. When the results of RT-PCR were compared with the conventional karyotype, the fusion was present in 3 of 10 (33%) with chromosome 12 abnormalities, none of whom had an obvious t(12;21). The transcript was also detected in 5 of the 12 (41%) bone marrow samples with other abnormalities and in 1 of 12 (8%) samples with a normal karyotype. Seven of the 9 RT-PCR positive patient samples were studied with FISH. Of the 7, FISH confirmed the ETV6/CBFA2 fusion in 6. One other patient with a 12p abnormality had evidence for the fusion using FISH which was not detected by RT-PCR. Our results not only confirm that the frequency of the t(12;21) is unusually high in childhood B-cell precursor ALL, but also that none of the translocations in our series was detected with conventional cytogenetic techniques.

摘要

最近发现的ETV6/CBFA2(以前称为TEL/AML1)融合基因是由t(12;21)(p12;q22)导致的。初步报告表明,融合转录本在高达30%被诊断为B细胞前体(CD10+、CD19+)急性淋巴细胞白血病(ALL)的儿童中出现。为了在染色体水平以及RNA转录本水平上确定t(12;21)的发生率,我们结合使用经典细胞遗传学、逆转录聚合酶链反应(RT-PCR)和荧光原位杂交(FISH)来检测34名被诊断为B细胞前体ALL的儿童的骨髓。34例患者样本中有9例表达了ETV6/CBFA2转录本。当将RT-PCR结果与传统核型进行比较时,在10例(33%)有12号染色体异常的患者中,有3例存在融合,其中无一例有明显的t(12;21)。在12例(41%)有其他异常的骨髓样本中以及12例(8%)核型正常的样本中也检测到了该转录本。对9例RT-PCR阳性患者样本中的7例进行了FISH研究。在这7例中,FISH在6例中证实了ETV6/CBFA2融合。另一名有12p异常的患者通过FISH有融合证据,但RT-PCR未检测到。我们的结果不仅证实了t(12;21)在儿童B细胞前体ALL中的频率异常高,而且我们系列中的所有易位均未通过传统细胞遗传学技术检测到。

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